Deferasorox

Product NDC
69539-200
11-digit product format
695390200
Labeler code
69539
Product ID
69539-200_40154b92-b71c-4ccc-b959-99b5c1528d25
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Deferasirox
Dosage form
GRANULE
Route
ORAL
Labeler
MSN LABORATORIES PRIVATE LIMITED
Application
ANDA214650
Marketing category
ANDA
Marketing start
2021-03-18
Marketing end
0000-00-00
Substance
DEFERASIROX
Active strength
360 mg/1
Pharmacologic classes
Cytochrome P450 1A2 Inhibitors [MoA], Cytochrome P450 2C8 Inhibitors [MoA], Cytochrome P450 3A4 Inducers [MoA], Iron Chelating Activity [MoA], Iron Chelator [EPC]
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69539-200DEFERASOROX (DEFERASIROX) GRANULE [MSN LABORATORIES PRIVATE LIMITED]2Legacy NDC20220503_97a62d3d-b910-4d2d-abf6-19ffa33e7005.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
69539-200-306953902003030 PACKET in 1 CARTON (69539-200-30) > 1 GRANULE in 1 PACKET (69539-200-62) 30 packet2021-03-180000-00-00NoNoCurrent